Allen S - Search Results

1

Cell-Free DNA in the Investigation of Miscarriage.

Colley E, Devall AJ, Williams H, Hamilton S, Smith P, Morgan NV, Quenby S, Coomarasamy A, Allen S. Colley E, et al. Among authors: allen s. J Clin Med. 2020 Oct 26;9(11):3428. doi: 10.3390/jcm9113428. J Clin Med. 2020. PMID: 33114508 Free PMC article.

2

Implementation and experience of an alternative QF-PCR and MLPA diagnostic strategy to detect chromosomal abnormalities in fetal and neonatal pathology samples.

McClelland LS, Allen SK, Larkins SA, Hamilton SJ, Marton T, Cox PM, Hargitai B, Johnston EH, Morgan C, Hardy G. McClelland LS, et al. Among authors: allen sk. Pediatr Dev Pathol. 2011 Nov-Dec;14(6):460-8. doi: 10.2350/11-01-0971-OA.1. Epub 2011 Aug 29. Pediatr Dev Pathol. 2011. PMID: 21875355

3

Chromosomal microarray analysis allows prenatal detection of low level mosaic autosomal aneuploidy.

Hall GK, Mackie FL, Hamilton S, Evans A, McMullan DJ, Williams D, Allen S, Kilby MD. Hall GK, et al. Among authors: allen s. Prenat Diagn. 2014 May;34(5):505-7. doi: 10.1002/pd.4333. Epub 2014 Feb 14. Prenat Diagn. 2014. PMID: 24464918 No abstract available.

4

Prenatal central nervous system anomaly with skeletal dysplasia associated with a de novo interstitial tandem triplication of chromosome 14.

Hall GK, Mackie FL, Williams H, Williams D, Cox P, McMullan DJ, Allen S, Kilby MD. Hall GK, et al. Among authors: allen s. J Obstet Gynaecol. 2017 Apr;37(3):375-376. doi: 10.1080/01443615.2016.1217513. Epub 2016 Dec 28. J Obstet Gynaecol. 2017. PMID: 28029058 No abstract available.

5

Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.

Colley E, Hamilton S, Smith P, Morgan NV, Coomarasamy A, Allen S. Colley E, et al. Among authors: allen s. Hum Reprod Update. 2019 Jul 1;25(4):452-472. doi: 10.1093/humupd/dmz015. Hum Reprod Update. 2019. PMID: 31150545

6

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.

Chong HP, Hamilton S, Mone F, Cheung KW, Togneri FS, Morris RK, Quinlan-Jones E, Williams D, Allen S, McMullan DJ, Kilby MD. Chong HP, et al. Among authors: allen s. Prenat Diagn. 2019 Nov;39(12):1064-1069. doi: 10.1002/pd.5545. Epub 2019 Aug 22. Prenat Diagn. 2019. PMID: 31393021

7

Evolution of a prenatal genetic clinic-A 10-year cohort study.

Mone F, O'Connor C, Hamilton S, Quinlan-Jones E, Allen S, Marton T, Williams D, Kilby MD. Mone F, et al. Among authors: allen s. Prenat Diagn. 2020 Apr;40(5):618-625. doi: 10.1002/pd.5661. Epub 2020 Feb 21. Prenat Diagn. 2020. PMID: 32037575

8

Diagnostic and perinatal outcomes in consanguineous couples with a structural fetal anomaly: A cohort study.

Mone F, Doyle S, Ahmad A, Abu Subieh H, Hamilton S, Allen S, Marton T, Williams D, Kilby MD. Mone F, et al. Among authors: allen s. Acta Obstet Gynecol Scand. 2021 Mar;100(3):418-424. doi: 10.1111/aogs.14036. Epub 2020 Nov 27. Acta Obstet Gynecol Scand. 2021. PMID: 33128783 Free article.

9

Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing Strategies.

Gerrish A, Bowns B, Mashayamombe-Wolfgarten C, Young E, Court S, Bott J, McCalla M, Ramsden S, Parks M, Goudie D, Carless S, Clokie S, Cole T, Allen S. Gerrish A, et al. Among authors: allen s. J Clin Med. 2020 Oct 30;9(11):3517. doi: 10.3390/jcm9113517. J Clin Med. 2020. PMID: 33143217 Free PMC article.

10

The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study.

Mone F, Stott BK, Hamilton S, Seale AN, Quinlan-Jones E, Allen S, Hurles ME, McMullan DJ, Maher ER, Kilby MD. Mone F, et al. Among authors: allen s. Fetal Diagn Ther. 2021 Feb 5:1-8. doi: 10.1159/000512488. Online ahead of print. Fetal Diagn Ther. 2021. PMID: 33550297

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